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FDA 510(k)

SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD

K-Number: K844761 · 1984-12-24

Decision Date1984-12-24
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instrument Development Laboratories, Inc.. It received FDA 510(k) clearance on 1984-12-24 under 510(k) number K844761. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD?

SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD is a medical device that received FDA 510(k) clearance on 1984-12-24. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K844761.

When did SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD receive FDA 510(k) clearance?

SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD received FDA 510(k) clearance on 1984-12-24, under 510(k) number K844761.

Who is the listed applicant for SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD?

The FDA 510(k) record lists Medical Instrument Development Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD?

The FDA product code for SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD is HOY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medical Instrument Development Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 22 devices →

Related Devices (Code: HOY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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